TY - JOUR
T1 - Lead-free cesium titanium bromide double perovskite nanocrystals
AU - Grandhi, G. Krishnamurthy
AU - Matuhina, Anastasia
AU - Liu, Maning
AU - Annurakshita, Shambhavee
AU - Ali-Löytty, Harri
AU - Bautista, Godofredo
AU - Vivo, Paola
PY - 2021/6
Y1 - 2021/6
N2 - Double perovskites are a promising family of lead-free materials that not only replace lead but also enable new optoelectronic applications beyond photovoltaics. Recently, a titanium (Ti)-based vacancy-ordered double perovskite, Cs2 TiBr6, has been reported as an example of truly sustainable and earth-abundant perovskite with controversial results in terms of photoluminescence and environmental stability. Our work looks at this material from a new perspective, i.e., at the nanoscale. We demonstrate the first colloidal synthesis of Cs2 TiX6 nanocrystals (X = Br, Cl) and observe tunable morphology and size of the nanocrystals according to the set reaction temperature. The Cs2 TiBr6 nanocrystals synthesized at 185◦ C show a bandgap of 1.9 eV and are relatively stable up to 8 weeks in suspensions. However, they do not display notable photoluminescence. The centrosymmetric crystal structure of Cs2 TiBr6 suggests that this material could enable third-harmonic generation (THG) responses. Indeed, we provide a clear evidence of THG signals detected by the THG microscopy technique. As only a few THG-active halide perovskite materials are known to date and they are all lead-based, our findings promote future research on Cs2 TiBr6 as well as on other lead-free double perovskites, with stronger focus on currently unexplored nonlinear optical applications.
AB - Double perovskites are a promising family of lead-free materials that not only replace lead but also enable new optoelectronic applications beyond photovoltaics. Recently, a titanium (Ti)-based vacancy-ordered double perovskite, Cs2 TiBr6, has been reported as an example of truly sustainable and earth-abundant perovskite with controversial results in terms of photoluminescence and environmental stability. Our work looks at this material from a new perspective, i.e., at the nanoscale. We demonstrate the first colloidal synthesis of Cs2 TiX6 nanocrystals (X = Br, Cl) and observe tunable morphology and size of the nanocrystals according to the set reaction temperature. The Cs2 TiBr6 nanocrystals synthesized at 185◦ C show a bandgap of 1.9 eV and are relatively stable up to 8 weeks in suspensions. However, they do not display notable photoluminescence. The centrosymmetric crystal structure of Cs2 TiBr6 suggests that this material could enable third-harmonic generation (THG) responses. Indeed, we provide a clear evidence of THG signals detected by the THG microscopy technique. As only a few THG-active halide perovskite materials are known to date and they are all lead-based, our findings promote future research on Cs2 TiBr6 as well as on other lead-free double perovskites, with stronger focus on currently unexplored nonlinear optical applications.
KW - Double perovskites
KW - Lead-free halide perovskites
KW - Nanocrystals
KW - Nonlinear optics
KW - Stability
KW - Third-harmonic generation
KW - Titanium (Ti)
U2 - 10.3390/nano11061458
DO - 10.3390/nano11061458
M3 - Article
AN - SCOPUS:85107016093
SN - 2079-4991
VL - 11
JO - Nanomaterials
JF - Nanomaterials
IS - 6
M1 - 1458
ER -